A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497533



Internal ID20870740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89064501..89303800hg38UCSC Ensembl
chr16:89130909..89370208hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38239300
hg19239300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178365
Samples
Known GenesACSF3, ANKRD11, CDH15, LINC00304, LOC400558, SLC22A31, ZNF778
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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